HMS-DHR-3 NEUROMUSCULAR STIMULATOR— 510(k) K021472

Name: FDA 510(k) clearance K021472
Creator: U.S. Food and Drug Administration
Published: 2002-08-06

Substantially Equivalent

Home Medical Services

FDA 510(k) clearance K021472 for HMS-DHR-3 NEUROMUSCULAR STIMULATOR, Substantially Equivalent on 2002-08-06. Applicant: Home Medical Services. Device class: 2.

Clearance details

Applicant: Home Medical Services
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2002-05-08
Decision date: 2002-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.